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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258235Generated: October 25, 2026

Diazald → Methyl deoxycholate

https://huagongshe.com/reaction/258235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiazaldHCID 6628—
ReactantDiazomethaneHCID 9550—
ReactantDeoxycholic AcidHCID 222528—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductMethyl deoxycholateHCID 229346—

Reaction Steps

Deoxycholic acid (0.54 g, 1.4 mmol) in THF (10 ml) at 0° C. was treated dropwise with freshly prepared diazomethane in ether (prepared in the usual manner from diazald) until the yellow colour persisted. After 15 minutes at 0° C. the solvent was evaporated to yield a white foam (0.60 g). The compound would not recrystallise, although gas chromatography showed the product to be 99% pure. The product was further purified by preparative silica tlc. (solvent system: EtOAc/CH2Cl2 /AcOH--10:10:1) to afford pure methyl deoxycholate2 (0.45 g, 80%) as a foam: 1H NMR (60 MHz; CDCl3) δ0.67 (3H, s, 18-CH3), 0.92 (3H, s, 18-CH3), 2.18 (2H, s [exchanges on adding D2O], 3α and 12α OH's), 3.2-3.7 (1H, m. 3β-H), 3.65 (3 H, s, --OMe), 3.8-4-1 (1H, m, 12β-H); IR (nujol mull) 3368 (OH's), 1740 (C=O) cm-1 ; MS: Found m/z 388.2951; C25H40O3 (M-H2O) requires 388.2977.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05266566
Source datasetuspto-grants-1993_11
ORD IDord-b0c15b2254654d1e958362c00ec2584b
Source noteuspto-grants-1993_11